Chromosomal Study is Must for Prepubertal Girl with Inguinal Hernia: Opportunity to Diagnose Complete Androgen Insensitivity Syndrome

• Main Authors: Sudipto Konar, Debdeep Dasgupta, Dipak Kumar Patra, Angshuman De, Barindranath Mallick
• Format: Article
• Language: English
• Published: JCDR Research and Publications Private Limited 2015-04-01
• Series: Journal of Clinical and Diagnostic Research
• Subjects: gonadectomy; karyotyping; male pseudohermaphroditism
• Online Access: https://jcdr.net/articles/PDF/5750/11411_CE[Ra1]_F(AK)_PF1(NJAK)_PFA(AK)_PF2(PAG).pdf

The sufferers of complete androgen insensitivity syndrome (CAIS) are phenotypic females despite of having functional testes and normal male karyotype. They usually present late with primary amenorrhea but delayed diagnosis increases chance of gonadal malignancy. Alertness for this entity is crucial as with early diagnosis such disorder can be managed more appropriately for a better future. We hereby describe a case of CAIS in an 8-year-old girl presented with bilateral inguinal swellings. Endocrinological analysis, radiological investigations and cytogenetic studies were done. Investigations revealed absence of female internal genitalia. Karyotyping and molecular study confirmed the presence of Y chromosome. Parents were counseled regarding timely gonadectomy, fertility and other long term social issues.